Hyperbranched Cationic Polymer for Graphene Packaging Adhesion

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing binders for graphene packaging materials have low adhesive strength, high manufacturing costs, and unchangeable adhesive strength, leading to poor bonding between graphene and polymer substrates, which affects the safety and barrier properties of drug packaging.

Innovation Solution

A hyperbranched cationic mussel-imitated polymer is developed using the reversible addition fragmentation chain transfer (RAFT) polymerization method with multi-hydroxylbenzoylbenzamide ene amide, cationic, and photo-responsive monomers, incorporating free catechol and cationic groups for enhanced intermolecular forces and adjustable bonding strength through fluorine substitution.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Strength

If existing binders are used to bond graphene film material and polymer film substrate, then the bonding process is simple, but the adhesive strength is low and bonding strength is poor

Engineering Contradiction:
Improveadhesive strengthVSAvoidbinder structure complexity
Core Design Contradiction:
StrengthVSDevice complexity

Solution Approach 1:

The invention uses a composite binder system containing both catechol groups (for metal coordination and hydrogen bonding) and cationic groups (for electrostatic interaction with graphene). This multi-functional composite structure enables strong adhesion to both graphene and polymer substrates simultaneously, resolving the low adhesive strength problem while maintaining reasonable structural complexity through the use of dendritic polymer architecture.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The invention changes the chemical parameters of the binder by incorporating specific functional groups (catechol and cationic groups) in controlled ratios. The catechol groups provide strong coordination bonds with metal atoms on graphene surface, while cationic groups enhance electrostatic interaction. This parameter optimization achieves high adhesive strength without excessive structural complexity.

Inventive Principle:
Principle #35Parameter changes

2Adaptability or versatility

If existing binders are used for graphene packaging, then manufacturing cost is high, but adhesive strength cannot be adjusted

Engineering Contradiction:
Improveadhesive strength adjustabilityVSAvoidmanufacturing cost
Core Design Contradiction:
Adaptability or versatilityVSEase of manufacture

Solution Approach 1:

The invention creates a dynamic binder system where the adhesive strength can be adjusted by modifying the ratio of catechol groups to cationic groups in the polymer structure. This allows the binder to be adapted to different packaging requirements (different levels of adhesion needed) while using the same basic polymer framework, reducing manufacturing costs through a versatile platform approach rather than developing multiple different binders.

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

By changing the compositional parameters (ratio of functional groups, molecular weight, branching degree) of the dendritic polymer, the adhesive strength can be tuned to match specific packaging applications. This parameter adjustment capability provides versatility without requiring completely different binder formulations for different applications, thereby controlling manufacturing costs.

Inventive Principle:
Principle #35Parameter changes

3Strength

If existing binders are used to bond graphene, then the contact area is small and reaction sites are few, but the bonding strength is poor

Engineering Contradiction:
Improvebonding strengthVSAvoidcontact area
Core Design Contradiction:
StrengthVSArea of stationary object

Solution Approach 1:

The dendritic polymer structure naturally segments the binder into multiple branching units, each containing reactive functional groups. This segmentation increases the number of contact points and reaction sites between the binder and graphene surface. The multi-branched architecture provides numerous catechol and cationic groups distributed throughout the polymer structure, enabling simultaneous bonding at multiple locations rather than relying on a single contact area.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The invention changes the structural parameters of the binder by using dendritic architecture with controlled branching degrees and functional group densities. This increases the effective contact area and number of reaction sites with graphene without requiring a proportional increase in binder quantity. The optimized parameter combination achieves high bonding strength through increased interfacial interaction density.

Inventive Principle:
Principle #35Parameter changes

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The hyperbranched polymer exhibits improved adhesive properties, adjustable binding strength, and reduced manufacturing costs, significantly enhancing the safety and barrier properties of graphene-based packaging materials.

Implementation Method 1

a large amount of free catechol groups and cationic groups of the R2 in formula (I) allows the hyperbranched polymer to have good adhesive properties to different substrates through a series of intermolecular forces with the different strength such as van der Waals force, hydrogen bonding, the interacting force between cationic and pi

Methodology Applied
Scientific EffectHydrogen bonding:

Implementation Method 2

a series of intermolecular forces with the different strength such as van der Waals force, hydrogen bonding, the interacting force between cationic and pi

Methodology Applied
Scientific Effectvan der Waals force: Van der Waals Force

Implementation Method 3

the interacting force between cationic and pi

Methodology Applied
Scientific EffectCationic-pi interaction:

Implementation Method 4

the benzene ring radical may attack the C—H bond on the graphene molecule and chemically react to form the covalent bond

Methodology Applied
Scientific EffectCovalent bonding: Chemical Bonding

Implementation Method 5

the inventors uses the reversible addition fragmentation chain transfer (RAFT) polymerization method which uses a multi-hydroxylbenzoylbenzamide ene amide monomer, a cationic monomer, a photo-responsive monomer

Methodology Applied
Scientific EffectRAFT polymerization:

Implementation Method 6

the cationic end groups can enhance the bonding force of the catechol groups to various substrates through synergistic effect. Moreover, as shown in formula (II), the groups of R3, R4, R5 and R6 in R1 can partially or totally be halogen which may generate a benzene ring radical under the action of light

Methodology Applied
Scientific EffectPhoto-responsive reaction:

Data Source

PatentUS10703835B2Hyperbranched cationic mussel-imitated polymer and method of preparing the same
Publication Date: 2020.07.07 SICHUAN HUILI IND
  • US10703835B2 patent drawing
  • US10703835B2 patent drawing
  • US10703835B2 patent drawing

AI summary

The present invention discloses a hyperbranched cationic mussel-imitated polymer and a method of preparing the same. The hyperbranched polymer disclosed in the present invention has the excellent mussel-imitated non-selective adhesive property, good biocompatibility and adhesive strength adjustability. The method of the present invention includes the following steps: (A) adding an initiator, a RAFT agent and a first reaction mixture to a vessel containing DMF to form a second reaction mixture; (B) stirring the second reaction mixture until homogenous, and introducing argon to a reaction system to remove oxygen in the reaction system; (C) heating and stirring the second reaction mixture to carry out a reaction; (D) after a product with a desired molecular weight being produced, the reaction system being exposed to air and cooled rapidly in a cold water bath to terminate the reaction; and (E) purifying the product to obtain the hyperbranched cationic mussel-imitated polymer.